Marfan syndrome is due to a mutation in a gene that encodes aprotein called fibrillin-1. It is inherited as a dominant trait. Thefibrillin-1 protein is the main constituent of extracellular microfibrils.These microfibrils can exist as individual fibers or associatewith a protein called elastin to form elastic fibers. People with thedisorder tend to be unusually tall with long limbs, and they mayhave defects in their heart valves and aorta. Let’s suppose aphenotypically unaffected woman has a child with a man whohas Marfan syndrome.A. What is the probability this child will have the disease?B. If this couple has three children, what is the probability thatnone of them will have Marfan syndrome?
Marfan syndrome is due to a mutation in a gene that encodes a
protein called fibrillin-1. It is inherited as a dominant trait. The
fibrillin-1 protein is the main constituent of extracellular microfibrils.
These microfibrils can exist as individual fibers or associate
with a protein called elastin to form elastic fibers. People with the
disorder tend to be unusually tall with long limbs, and they may
have defects in their heart valves and aorta. Let’s suppose a
has Marfan syndrome.
A. What is the probability this child will have the disease?
B. If this couple has three children, what is the probability that
none of them will have Marfan syndrome?
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